JPS5896006A - 除草剤と、除草剤間の活性「あ」抗を阻止する方法 - Google Patents
除草剤と、除草剤間の活性「あ」抗を阻止する方法Info
- Publication number
- JPS5896006A JPS5896006A JP57200250A JP20025082A JPS5896006A JP S5896006 A JPS5896006 A JP S5896006A JP 57200250 A JP57200250 A JP 57200250A JP 20025082 A JP20025082 A JP 20025082A JP S5896006 A JPS5896006 A JP S5896006A
- Authority
- JP
- Japan
- Prior art keywords
- herbicide
- composition
- crop oil
- amount
- pyridyloxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004009 herbicide Substances 0.000 title claims abstract description 67
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 51
- 230000002265 prevention Effects 0.000 title description 2
- 239000005557 antagonist Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 47
- REEXLQXWNOSJKO-UHFFFAOYSA-N 2h-1$l^{4},2,3-benzothiadiazine 1-oxide Chemical compound C1=CC=C2S(=O)NN=CC2=C1 REEXLQXWNOSJKO-UHFFFAOYSA-N 0.000 claims abstract description 22
- 230000008485 antagonism Effects 0.000 claims abstract description 11
- 241000196324 Embryophyta Species 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 9
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical group OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 claims description 7
- 239000007921 spray Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 230000003405 preventing effect Effects 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical group COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 claims 1
- 235000019260 propionic acid Nutrition 0.000 claims 1
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 claims 1
- 239000003921 oil Substances 0.000 description 42
- 150000001875 compounds Chemical class 0.000 description 8
- 239000012141 concentrate Substances 0.000 description 8
- 238000009472 formulation Methods 0.000 description 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 4
- 230000003115 biocidal effect Effects 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 241000209504 Poaceae Species 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- -1 alkali metal salts Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 208000012766 Growth delay Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 235000005775 Setaria Nutrition 0.000 description 1
- 241000232088 Setaria <nematode> Species 0.000 description 1
- 235000002248 Setaria viridis Nutrition 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- BTMVHUNTONAYDX-UHFFFAOYSA-N butyl propionate Chemical compound CCCCOC(=O)CC BTMVHUNTONAYDX-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 108010011222 cyclo(Arg-Pro) Proteins 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 244000230342 green foxtail Species 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- MFSWTRQUCLNFOM-UHFFFAOYSA-N methyl 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical compound C1=CC(OC(C)C(=O)OC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl MFSWTRQUCLNFOM-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
- A01N61/02—Mineral oils; Tar oils; Tar; Distillates, extracts or conversion products thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US321352 | 1981-11-16 | ||
| US06/321,352 US4447257A (en) | 1981-11-16 | 1981-11-16 | Inhibiting the antagonism between pyridyloxy-phenoxy alkanoate herbicides and benzothiadiazinone herbicides in post-emergent applications |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5896006A true JPS5896006A (ja) | 1983-06-07 |
Family
ID=23250255
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57200250A Pending JPS5896006A (ja) | 1981-11-16 | 1982-11-15 | 除草剤と、除草剤間の活性「あ」抗を阻止する方法 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4447257A (en:Method) |
| EP (1) | EP0079774B1 (en:Method) |
| JP (1) | JPS5896006A (en:Method) |
| AT (1) | ATE15580T1 (en:Method) |
| AU (1) | AU555037B2 (en:Method) |
| BR (1) | BR8206633A (en:Method) |
| CA (1) | CA1186908A (en:Method) |
| DE (1) | DE3266427D1 (en:Method) |
| DK (1) | DK157285C (en:Method) |
| GB (1) | GB2111389B (en:Method) |
| GR (1) | GR77759B (en:Method) |
| IL (1) | IL67175A (en:Method) |
| MY (1) | MY8700324A (en:Method) |
| NZ (1) | NZ202498A (en:Method) |
| ZA (1) | ZA828142B (en:Method) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01261312A (ja) * | 1988-02-27 | 1989-10-18 | Hoechst Ag | 水性マイクロエマルジョンの形態の除草剤 |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4824475A (en) * | 1985-09-16 | 1989-04-25 | The Dow Chemical Company | Enhanced herbicidal triazine compositions and method of use |
| US5102442A (en) * | 1987-10-05 | 1992-04-07 | Basf Corporation | Antagonism defeating crop oil concentrates |
| US4834908A (en) * | 1987-10-05 | 1989-05-30 | Basf Corporation | Antagonism defeating crop oil concentrates |
| US5238604A (en) * | 1987-10-05 | 1993-08-24 | Basf Corporation | Crop oil concentrates |
| AP112A (en) * | 1988-03-16 | 1990-03-05 | Ici South Africa Ltd | Herbicides. |
| US5084087A (en) * | 1989-04-26 | 1992-01-28 | Basf Corporation | Ready to dilute adjuvant-containing postemergent herbicide formulations |
| US6218337B1 (en) * | 1996-09-27 | 2001-04-17 | Basf Aktiengesellschaft | Solid mixtures of 3-isopropyl-2,1,3-benzothiadiazin-4-one-2,2,-dioxide or its salts |
| CA2607618C (en) * | 2005-05-10 | 2014-09-16 | Syngenta Participations Ag | Herbicidal compositions |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3997322A (en) * | 1970-09-09 | 1976-12-14 | Sun Oil Company Of Pennsylvania | Herbicide carrier oil composition |
| JPS54119476A (en) * | 1978-03-10 | 1979-09-17 | Ishihara Sangyo Kaisha Ltd | 4-(5-fluoromethyl-2-pyridyloxy)phenoxyalkanecarbocyic acid derivatives and their preparation |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3041336A (en) * | 1958-10-01 | 1962-06-26 | Norwich Pharma Co | 3-oxo-1.2.6-thiadiazine-1.1-dioxides |
| US3217001A (en) * | 1963-08-19 | 1965-11-09 | American Home Prod | Derivatives of 1h-2, 1, 3-benzothiadiazin-4(3h)-one 2-oxide and intermediates therefor |
| US3708277A (en) * | 1966-08-30 | 1973-01-02 | Basf Ag | Herbicidal method |
| US3621017A (en) * | 1967-09-30 | 1971-11-16 | Basf Ag | Salts of thiadiazinones |
| NL7302541A (en:Method) * | 1972-02-28 | 1973-08-30 | ||
| US3940389A (en) * | 1973-09-17 | 1976-02-24 | The Dow Chemical Company | 4 (3H)-Oxobenzo-2,1,3-thiadiazine-2,2-dioxides |
| US4051130A (en) * | 1974-08-15 | 1977-09-27 | The Dow Chemical Company | 4(3H)-oxobenzo-2,1,3-thiadiazine-2,2-dioxides and derivatives thereof |
| US4155746A (en) * | 1976-01-15 | 1979-05-22 | The Dow Chemical Company | Postemergent herbicidal method using 8-substituted benzothiadiaziones |
| US4116672A (en) * | 1976-03-12 | 1978-09-26 | The Dow Chemical Company | 4(3H)-Oxobenzo-2,1,3-thiadiazine-2,2-dioxides and derivatives thereof |
| CA1247625A (en) * | 1977-07-22 | 1988-12-28 | Howard Johnston | Trifluoromethyl pyridinyloxyphenoxy propanoic acids and propanols and derivatives thereof and methods of herbicidal use |
| GB1550574A (en) * | 1977-12-12 | 1979-08-15 | Ciba Geigy Ag | Pyridyloxy-phenoxy-propionic acid derivatives which are effective as herbicides and as agents regulating plant growth |
| DE2960106D1 (en) * | 1978-01-27 | 1981-02-26 | Ciba Geigy Ag | Aminoalkyl esters of pyridyloxy-phenoxy-alpha-propionic acids with herbicidal activity, their preparation, compositions containing them and their application |
| DE2967486D1 (en) * | 1978-03-01 | 1985-08-29 | Ici Plc | Mixtures of herbicidal pyridyloxyphenoxypropanoic acid derivatives with other herbicides, and processes of killing unwanted plants therewith |
-
1981
- 1981-11-05 ZA ZA828142A patent/ZA828142B/xx unknown
- 1981-11-16 US US06/321,352 patent/US4447257A/en not_active Expired - Fee Related
-
1982
- 1982-10-29 CA CA000414519A patent/CA1186908A/en not_active Expired
- 1982-11-03 IL IL67175A patent/IL67175A/xx unknown
- 1982-11-04 DK DK489382A patent/DK157285C/da active
- 1982-11-04 AU AU90162/82A patent/AU555037B2/en not_active Ceased
- 1982-11-12 DE DE8282306033T patent/DE3266427D1/de not_active Expired
- 1982-11-12 BR BR8206633A patent/BR8206633A/pt unknown
- 1982-11-12 EP EP82306033A patent/EP0079774B1/en not_active Expired
- 1982-11-12 GB GB08232339A patent/GB2111389B/en not_active Expired
- 1982-11-12 AT AT82306033T patent/ATE15580T1/de not_active IP Right Cessation
- 1982-11-15 NZ NZ202498A patent/NZ202498A/xx unknown
- 1982-11-15 JP JP57200250A patent/JPS5896006A/ja active Pending
- 1982-11-16 GR GR69833A patent/GR77759B/el unknown
-
1987
- 1987-12-30 MY MY324/87A patent/MY8700324A/xx unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3997322A (en) * | 1970-09-09 | 1976-12-14 | Sun Oil Company Of Pennsylvania | Herbicide carrier oil composition |
| JPS54119476A (en) * | 1978-03-10 | 1979-09-17 | Ishihara Sangyo Kaisha Ltd | 4-(5-fluoromethyl-2-pyridyloxy)phenoxyalkanecarbocyic acid derivatives and their preparation |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01261312A (ja) * | 1988-02-27 | 1989-10-18 | Hoechst Ag | 水性マイクロエマルジョンの形態の除草剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1186908A (en) | 1985-05-14 |
| ZA828142B (en) | 1984-06-27 |
| GB2111389A (en) | 1983-07-06 |
| EP0079774B1 (en) | 1985-09-18 |
| DK157285C (da) | 1990-05-07 |
| US4447257A (en) | 1984-05-08 |
| AU555037B2 (en) | 1986-09-11 |
| DK489382A (da) | 1983-05-17 |
| NZ202498A (en) | 1985-05-31 |
| IL67175A (en) | 1985-11-29 |
| AU9016282A (en) | 1983-05-26 |
| DK157285B (da) | 1989-12-04 |
| BR8206633A (pt) | 1983-10-04 |
| DE3266427D1 (en) | 1985-10-24 |
| EP0079774A1 (en) | 1983-05-25 |
| MY8700324A (en) | 1987-12-31 |
| GB2111389B (en) | 1985-06-05 |
| IL67175A0 (en) | 1983-03-31 |
| GR77759B (en:Method) | 1984-09-25 |
| ATE15580T1 (de) | 1985-10-15 |
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